HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Diisopropyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dichloroisoquinoline-7-sulfonyl chloride | HCID 16658294 | — |
| Reactant | Nalpha-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-Nepsilon-tert-butyloxycarbonyl-L-lysine tert-butyl ester | HCID 21969824 | — |
| Reactant | 7750-45-0 | HCID 51358437 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diisopropyl Ether | HCID 7914 | — |
| Product | Nalpha-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-Nepsilon-tert-butyloxycarbonyl-L-lysine tert-butyl ester | HCID 21969824 | — |
Reaction Steps
Nα-[(1,4-Dichloro-7-isoquinolinyl)sulphonyl]-Nε-tert-butyloxycarbonyl-L-lysine tert-butyl ester ##STR190## A solution of 1,4-dichloro-7-isoquinolinylsulphonyl chloride (250 mg, 0.84 mmol), Ne-tert-butyloxycarbonyl-L-lysine tert-butyl ester hydrochloride (286 mg, 0.84 mmol) and triethylamine (235 μl, 1.69 mmol) in CH2Cl2 (25 ml) was stirred at 23° C. for 3h. The reaction mixture was washed with water (2×20 ml), dried (MgSO4) and concentrated in vacuo to a residue which upon trituration with hexane and then i-Pr2O gave Nα-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-Nε-tert-butyloxycarbonyl-L-lysine tert-butyl ester as a white powder (270 mg, 0.48 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093731 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-f0bce4b963bb48e8bdb4bbce261066aa |
| Source note | uspto-grants-2000_07 |